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greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks o...

FDA Recall #Z-1583-2023 — Class II — March 31, 2023

Recall #Z-1583-2023 Date: March 31, 2023 Classification: Class II Status: Completed

Product Description

greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003

Reason for Recall

Some of the tubes may be incorrectly labeled.

Recalling Firm

Greiner Bio-One North America, Inc. — Monroe, NC

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

36,000 pieces (30 full cases)

Distribution

US Nationwide distribution in the states of WI and GA.

Code Information

Lot #B220533J, Exp. 2023-10-31, UDI Case label (01)39120017576496(17)231031(10)B220533J, UDI Rack label 29120017576499(17)231031(10)B220533J.

Status

Completed

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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